Human netrin-1

ABSTRACT

Specific netrin proteins, nucleic acids which encode netrin proteins and hybridization reagents, probes and primers capable of hybridizing with netrin genes and methods for screening chemical libraries for lead compounds for pharmacological agents useful in the diagnosis or treatment of disease associated undesirable cell growth are provided. An exemplary screen involves forming a mixture comprising a recombinant netrin protein, a natural intracellular netrin protein binding target, and a candidate pharmacological agent; incubating the mixture under conditions whereby, but for the presence of said candidate pharmacological agent, said netrin protein selectively binds said binding target; and detecting the presence or absence of specific binding of said netrin protein to said binding target.

INTRODUCTION

1. Field of the Invention

The field of this invention is human netrin proteins and genes.

2. Background

In the developing nervous system, axons project considerable distances along stereotyped pathways to reach their targets. Axon growth and guidance depends partly on the recognition of cell-surface and extracellular matrix cues along these pathways. The identification of such nerve cell growth and guidance cues is the holy grail of neurobiology. These are the compounds that tell neurons when to grow, where to grow, and when to stop growing. The medical applications of such compounds are enormous and include modulating neuronal growth regenerative capacity, treating neurodegenerative disease, and mapping (e.g. diagnosing) genetic neurological defects.

Over decades of concentrated research, various hypotheses involving chemo-attractants and repellents, labeled pathways, cell adhesion molecules, etc. have been invoked to explain guidance. Molecules such as N-CAM and N-cadherin have been reported to provide favorable substrates for axon growth and certain sensory axons may be responsive to NGF and NGF-like factors. Recent reports suggest the existence of diffusible chemotropic molecule(s) which influence the pattern and orientation of commissural axon growth.

RELEVANT LITERATURE

Ishii et al. (1992) Neuron 9, 873-881 disclose a gene, unc-6, derived from C. elegans, which has sequence similarity to the disclosed netrins. Serafini et al (1994) Cell 78, 409-424 and Kennedy et al (1994) Cell 78, 425-435 at page 5, column 1 describe related vertebrate netrins. The work was also reported in The New York Times, Section B7, Tuesday, Aug. 16, 1994 and more recently (May 19, 1995) described in Science 268, 971-973 (see also references cited therein).

SUMMARY OF THE INVENTION

The invention provides methods and compositions relating to a human netrin protein and gene. Netrins are a class of proteins which are naturally involved in neural axon guidance. The subject compositions include nucleic acids which encode the specified netrin protein and hybridization probes and primers capable of hybridizing with the specified netrin gene. The netrin proteins finds particular use in modulating neural axon outgrowth. The disclosed compositions also find use variously in screening chemical libraries for regulators of axon outgrowth and orientation, in genetic mapping, as probes for netrin genes, as diagnostic reagents for genetic neurological disease and in the production of specific cellular and animal systems for the development of neurological disease therapy.

DETAILED DESCRIPTION OF THE INVENTION

The invention provides methods and compositions relating to a human netrin-1 protein and gene; including methods and compositions for identifying, purifying, characterizing, and producing the subject proteins and for identifying, characterizing, cloning, expressing, inhibiting the expression of and amplifying the subject nucleic acids. The subject proteins may be incomplete translates of the disclosed netrin cDNA sequence or deletion mutants of the corresponding conceptual translates, which translates or deletion mutants have the human netrin-1 binding activity and specificity described herein. The netrins are isolated, partially pure or pure and are typically recombinantly produced. An "isolated" protein for example, is unaccompanied by at least some of the material with which it is associated in its natural state; generally constituting at least about 0.5%, preferably at least about 2%, and more preferably at least about 10% by weight of the total protein in a given sample; and a pure protein constitutes at least about 50%, preferably at least about 90%, and more preferably at least about 99% by weight of the total protein in a given sample. A wide variety of molecular and biochemical methods are available for generating and expressing the subject compositions, see e.g. Molecular Cloning, A Laboratory Manual (Sambrook, et al. Cold Spring Harbor Laboratory), Current Protocols in Molecular Biology (Eds. Ausubel, et al., Greene Publ. Assoc., Wiley-Interscience, NY) or that are otherwise known in the art.

The disclosed netrin compositions may be used to modulate axon outgrowth or guidance in situ or in vivo. For in vivo applications, the compositions are added to a retained physiological fluid such as blood or synovial fluid. For CNS administration, a variety of techniques are available for promoting transfer of the therapeutic across the blood brain barrier including disruption by surgery or injection, drugs which transiently open adhesion contact between CNS vasculature endothelial cells, and compounds which facilitate translocation through such cells. Netrins may also be amenable to direct injection or infusion, topical, intratracheal/nasal administration e.g. through aerosol, intraocularly, or within/on implants e.g. fibers e.g. collagen, osmotic pumps, grafts comprising appropriately transformed cells, etc. A particular method of administration involves coating, embedding or derivatizing fibers, such as collagen fibers, protein polymers, etc. with therapeutic proteins. Other useful approaches are described in Otto et al. (1989) J Neuroscience Research 22, 83-91 and Otto and Unsicker (1990) J Neuroscience 10, 1912-1921. Generally, the amount administered will be empirically determined, typically in the range of about 10 to 1000 μg/kg of the recipient and the concentration will generally be in the range of about 50 to 500 μg/ml in the dose administered. Other additives may be included, such as stabilizers, bactericides, etc. will be present in conventional amounts.

The invention provides netrin-specific binding agents including isolated binding targets such as membrane-bound netrin receptors and netrin-specific antibodies and binding agents identified in screens of natural and synthetic chemical libraries, and methods of identifying and making such agents, and their use in diagnosis, therapy and pharmaceutical development. Generally, netrin-specificity of the binding agent is shown by binding equilibrium constants. Such agents are capable of selectively binding the specified netrin, i.e. with an equilibrium constant at least about 10⁷ M⁻¹, preferably at least about 10⁸ M⁻¹, more preferably at least about 10⁹ M⁻¹. A wide variety of cell-based and cell-free assays may be used to demonstrate netrin-specific binding; preferred are rapid in vitro, cell-free assays such as mediating or inhibiting netrin-cell/protein binding, immunoassays, etc.

The invention also provides nucleic acids encoding the subject proteins, which nucleic acids may be part of netrin-expression vectors and may be incorporated into recombinant cells for expression and screening, transgenic animals for functional studies (e.g. the efficacy of candidate drugs for neural disease or injury), etc. and nucleic acid hybridization probes and replication/amplification primers having a disclosed netrin cDNA specific sequence. The hybridization probes contain a sequence common or complementary to the corresponding netrin gene sufficient to make the probe capable of specifically hybridizing to the corresponding netrin gene, and only to the corresponding netrin gene, in the presence of other netrin genes. Hence, the subject probes and primers are uniquely specific to the disclosed cDNA. Hybridization probes having in excess of 100 continuous bases of netrin gene sequence are generally capable of hybridizing to the corresponding netrin cDNA and remaining bound at a reduced final wash stringency of 0.2×SSC (0.9 M saline/0.09 M sodium citrate) and 0.1% SDS buffer at a temperature of 65° C.

The subject nucleic acids are isolated, meaning they comprise a sequence joined to a nucleotide other than that which it is joined to on a natural chromosome, and usually constitute at least about 0.5% , preferably at least about 2%, and more preferably at least about 5% by weight of total nucleic acid present in a given fraction. A pure nucleic acid constitutes at least about 50%, preferably at least about 90%, and more preferably at least about 95% by weight of total nucleic acid present in a given fraction. The subject nucleic acids find a wide variety of applications including use as translatable transcripts, hybridization probes, PCR primers, therapeutic nucleic acids, etc.; use in detecting the presence of netrin genes and gene transcripts, e.g. allele-specific oligonucleotide (ASO) probes use to identify wild-type and mutant netrin alleles in clinical and laboratory samples, in detecting or amplifying nucleic acids encoding other netrins, and in gene therapy applications, e.g. antisense oligonucleotides capable of inhibiting the intracellular expression of a targeted netrin transcript.

The invention provides efficient methods of identifying pharmacological agents or lead compounds for agents capable of mimicking or modulating netrin function (e.g. bioactive netrin deletion mutants and netrin peptides). A wide variety of screens may be used; for example, cell-based assays may be used for monitoring netrin function and in vitro binding assays may be used to identify netrin-specific binding agents. Kennedy et al. (1994) Cell 78, 425-435 describe a particularly convenient COS cell-based netrin expression assay. Preferred methods are amenable to automated, cost-effective high throughput screening of natural and synthetic chemical libraries for lead compounds. Identified reagents find use in the pharmaceutical industries for animal and human trials; for example, the reagents may be derivatized and rescreened in in vitro and in vivo assays to optimize activity and minimize toxicity for pharmaceutical development.

EXAMPLES

Human Netrin 1 (SEQ ID NO:2) and cDNA (SEQ ID NO:1).

We isolated chicken netrin 1 and 2 cDNAs as described in Serafini et al. (1974) Cell 78:409-424. Based on the chick netrin 1 and 2 cDNA sequences, we designed degenerate oligonucleotide primers and used these primers to amplify a cDNA encoding mouse netrin 1 from a murine cDNA library. We then isolated a human netrin cDNA using degenerate oligonucleotide primers constructed using amino acid sequences conserved in chick and mouse netrin sequences as a guide.

The starting material for PCR was 100 ng of human genomic DNA. Two rounds of PCR amplification were used. In the first round, the following program and conditions were used: 1. 94° C. 30 sec.; 2. 50° C. 45 sec; 3. 72° C., 1 minute; 4. go to 1, 30 times; 5. 4° C.; 6. end. In the second round of PCR amplification, nested PCR and the following conditions and program were used: 1. 94° C. 1 minute; 2. 42° C. 1 minute; 3. increments of 1° C. every 5 seconds to 72° C.; 4. 72° C. for 3 minutes; 5. go to 1, 2 times; 6. 94° C. for 1 minute; 7. 46° C. for 1 minute; 8. increments of 1° C. every 6 seconds until 72° C.; 9. 72° C. 2 minutes; 10. go to 6, 7 times; 11. 94° C. for 1 minute; 12. 55° C. for 1 minute; 13. 72° C. 2 minute; 14. go to 11, 24 times; 15. 94° C. for 1 minute; 16. 55° C. for 1 minute; 17. 72° C. for 10 minutes; 18. 4° C.; 19. end. PCR products were subcloned and individual clones containing inserts corresponding to human netrin sequence isolated using a Grunstein and Hogness screen (Sambrook, 1989). ³² P was incorporated into a probe using PCR with a portion of the mouse netrin-1 cDNA clone as a template. The final wash of the filters was at a reduced stringency of 1× SSC and 0.1% SDS at 65° C. (Sambrook et al., 1989). This screen isolated an approximately 140 base pair human netrin CDNA clone. This cDNA fragment was used to isolate a longer human netrin cDNA from a Human fetal brain cDNA library (Stratagene cat#936206). The ˜140 base pair human netrin cDNA was used as a template and ³² P incorporated into a human netrin cDNA probe using PCR. 1×10⁶ clones were screened at high stringency (Sambrook et al., 1989) identifying a single approximately 7 kb netrin cDNA (HBC-1, deposited with ATCC Jun. 7, 1995, as plasmid HN-1, deposit number 97204).

Sequence analysis determined that an EcoRI subclone of the 7 kb HBC-1 clone corresponded to a splice variant of human netrin-1. The first 1086 base pairs of sequence show high homology to mouse netrin-1 and the remaining 626 base pairs are highly divergent. A potential splice donor site is identified at the junction of the netrin and the divergent sequence. A clone that corresponds to the 3' end of human netrin-1 was isolated using reverse transcription and PCR with a 5' primer at position 999 of the human sequence and a 3' degenerate primer to the last 15 base pairs of the mouse netrin sequence. Three additional independent clones were isolated to confirm the sequence of the PCR reaction product. The region of overlap between this new clone and the HBC-1 Eco clone is 46 base pairs and is identical in sequence. To verify the overlap, an additional clone was isolated using a 5' primer at position 818 and a 3' primer at position 1582 of the human netrin-1 sequence. Two independent clones isolated using these primers confirm the structure of the cDNA. Finally, the sequence encoding the C-terminal 5 amino acids was confirmed. A primer was designed to a region within the 3' untranslated region that is conserved between chicken and mouse netrin-1. A PCR product was generated using this primer and a 5' primer in the human sequence at position 1568 and the sequence was verified.

RT-PCR procedures were as follows: fetal brain RNA (19-23 weeks) was obtained from Clontech. RT-PCR was performed using the GeneAmp Thermostable rTth Reverse Transcriptase RNA PCR Kit from Perkin Elmer. A hot start technique was used to denature the RNA by mixing 50 ng with 30 pmol degenerate primer deg-1, 1 μl 10× rTth Reverse Transcriptase Buffer (Perkin Elmer) and water in a total volume of 7.2 μl; this mixture was heated to 95° C. for 2 minutes, followed by a 5 minute incubation at 70° C. The reaction was cooled to 60° C. and reverse transcription was begun by adding a mixture containing 1 μl 10 mM MnCl₂, 1 μl rTth DNA polymerase (Perkin Elmer, 2.5 U), and 0.2 μl each 10 mM dATP, dCTP, dGTP, and dTTP . The 60° C. incubation was continued for 5 minutes, followed by two 5 minute incubations at 65° C. and 70° C. The reaction was then chilled on ice.

To amplify the human netrin-1 fragment by PCR, a mixture containing 2 μl DMSO, 3 μl 25 mM MgCl₂, 4 μl 10× Chelating Buffer (Perkin Elmer) and 34.5 μl water was added to the reverse transcription reaction. 30 pmol of a human netrin-specific primer, h-net-5'999, was added (0.5 μl) to the mixture and PCR was carried out in an MJ Research PTC-200 Peltier Thermal Cycler using the "Calculated" temperature control method and the following conditions: 1) 95° C. for 2 minutes; 2) 55° C. for 25 seconds; 3) 95° C. for 10 seconds; 4) Repeat steps 2-3, 34 times; 5) 60° C. for 7 minutes; and 6) 4° C. hold.

The reaction was analyzed by gel electrophoresis and transferred to nylon membrane. Netrin-specific products were detected by Southern hybridization using a mouse netrin probe corresponding to sequence from position 1342 to position 1875 of mouse netrin. A plug of agarose corresponding to the cross hybridizing fragment (migrating at approximately 850 bp) was extracted with a Pasteur pipet and reamplified as follows: the agarose plug was combined with a reaction mixture containing 1.25 μl formamide, 5 μl of 10× PCR Buffer II (Perkin Elmer), 5 μl of 25 mM MgCl₂, 30 pmol human netrin-specific primer h-net-5'999, 30 pmol degenerate netrin primer deg-1, 5 U AmpliTaq DNA Polymerase (Perkin Elmer), and sterile water in a total volume of 49 μl. PCR was carried out in an MJ Research PTC-200 Peltier Thermal Cycler using the "Block" temperature control method and the following conditions: 1) 95° C. for 2 minutes; 2) 50° C. for 1 minute; 3) 75° C. for 1 minute, 30 seconds; 4) 95° C. for 20 seconds; 5) Repeat steps 2-4, 39 times; 6) 75° C. for 10 minutes; and 7) 4° C. hold.

The reaction was analyzed by gel electrophoresis and a band of DNA at approximately 850 bp was purified using the BioRad Prep-A-Gene system, ligated with the TA cloning vector (InVitroGen), and transformed into DH5α competent bacterial cells. Colonies were analyzed for the correct size insert by colony PCR, grown overnight at 37° C. in LB media containing 100 μg/ml ampicillin, and DNA was prepared from the culture using a Qiagen Tip-100 column. The inserts were confirmed by restriction digests and the sequence was generated using an ABI 377 automated sequencer.

To confirm the last 15 nucleotides of the human netrin-1 clone, the 3' end of the clone was amplified from first strand cDNA using a 5' primer to known sequence and a 3' primer to sequence in the 3' untranslated region of the mouse netrin-1 clone. First, cDNA was synthesized as described in "Rapid Amplification of cDNA Ends," by Michael Frohman (In: PCR Primer: A Laboratory Manual, C. W. Dieffenbach and G. S. Dveksler, eds., Cold Spring Harbor Laboratory Press, 1995) using the protocol described in the section "3'-End cDNA Amplification" (pp. 388-389), and 1 μg fetal brain poly A+ RNA (Clontech). 1 μl of the diluted cDNA was amplified in a 50 μl reaction containing 67 mM Tris HCl, pH 9.0, 6.7 mM magnesium chloride, 16.6 mM ammonium sulfate, 0.17 mg/ml BSA, 10% DMSO, 1.5 mM each dNTP, 30 pmol 5'primer "h-net 5'1449" and 30 pmol 3' primer "m-net 3' UT 2238". The primer "h-net 5'1449" corresponds to sequence beginning at position 1449 in the human netrin-1 clone. The primer "m-net 3' UT 2238" corresponds to sequence in the 3' untranslated region of mouse netrin-1, with the addition of an Xba I restriction site sequence at the 5' end. Taq DNA polymerase, 1 μl, (Perkin Elmer) was combined with 0.5 μl TaqStart Antibody (ClonTech) and 2.5 μl TaqStart Antibody Dilution Buffer, incubated at room temperature for 10 minutes, and added to the PCR reaction mixture. The reaction was amplified in an MJ Research PTC-200 Peltier Thermal Cycler using the "Calculated" temperature control method and the following conditions: 1) 95° C. for 2 minutes; 2) 62° C. for 30 seconds; 3) 57° C. for 30 seconds; 4) 52° C. for 10 seconds; 5) 72° C. for 40 minutes; 6) 94° C. for 10 seconds; 7) 62° C. for 1 minute; 8) 72° C. for 3 minutes; 9) Repeat steps 6-8, 4 times; 10) 94° C. for 10 seconds; 11) 57° C. for 1 minute; 12) 72° C. for 3 minutes; 13) Repeat steps 10-12, 4 times; 14) 94° C. for 10 seconds; 15) 52° C. for 1 minute; 16) 72° C. for 3 minutes; 17) Repeat steps 14-16, 24 times; 18) 75° C. for 10 minutes; 19) 4° C. hold.

The reaction was diluted 1:20 in TE, and 1 μl was re-amplified in a 50 μl reaction containing 67 mM Tris HCl, pH 9.0, 6.7 mM magnesium chloride, 16.6 mM ammonium sulfate, 0.17 mg/ml BSA, 10% DMSO, 1.5 mM each dNTP, 30 pmol of the 5'primer "h-net 5'1702," 30 pmol of the 3'primer "m-net 3'UT 2238" and 0.25 ul Taq DNA Polymerase. The primer "m-net 5'1702" corresponds to sequence beginning at position 1568 in the human netrin-1 clone. The reaction was amplified in an MJ Research PTC-200 Peltier Thermal Cycler using the "Calculated" temperature control method and the following conditions: 1) 95° C. for 2 minutes; 2) 94° C. for 10 seconds; 3) 58° C. for 1 minute; 4) 72° C. for 3 minutes; 5) Repeat steps 2-4, 4 times; 6) 94° C. for 10 seconds; 7) 54° C. for 45 seconds; 8) 72° C. for 3 minutes; 9) Repeat steps 6-8, 4 times; 10) 94° C. for 10 seconds; 11) 50° C. for 30 seconds; 12) 72° C. for 3 minutes; 13) Repeat steps 10-12, 24 times; 14) 75° C. for 5 minutes; and 15) 4° C. hold.

The reaction was analyzed by gel electrophoresis and a 530 bp product was isolated from the gel using the Prep-A-Gene System (BioRad). The product was ligated into pCR 2.1 (InVitroGen) overnight at 14° C. Transformants were cultured overnight in LB media containing 100 μg/ml ampicillin and DNA was purified from cultures using Easy Pure Plasmid Preps (Super Mini, Primm Labs). DNA sequence was generated using an ABI 377 automated sequencer.

To confirm the 3' end sequence, two additional fragments spanning the 3' end of human netrin were generated by PCR using the m-net 5'1702 primer and a 3' primer, h-net 3'1959 corresponding to sequence in the 3' untranslated region of human netrin-1. Amplification with these primers generated products of approximately 390 base pairs in duplicate reactions. The fragments were amplified in an MJ Research PTC-200 Peltier Thermal Cycler using the "Calculated" temperature control method and the following conditions: 1) 95° C. for 2 minutes; 2) 94° C. for 10 seconds; 3) 58° C. for 1 minute; 4) 72° C. for 3 minutes; 5) Repeat steps 2-4, 4 times; 6) 94° C. for 10 seconds; 7) 54° C. for 45 seconds; 8) 72° C. for 3 minutes; 9) Repeat steps 6-8, 4 times; 10) 94° C. for 10 seconds; 11) 50° C. for 30 seconds; 12) 72° C. for 3 minutes; 13) Repeat steps 10-12, 19 times; 14) 75° C. for 5 minutes; and 15) 4° C. hold. The reactions were analyzed by gel electrophoresis to confirm their size, and directly sequenced using an ABI 377 automated sequencer.

All publications and patent applications cited in this specification are herein incorporated by reference as if each individual publication or patent application were specifically and individually indicated to be incorporated by reference. Although the foregoing invention has been described in some detail by way of illustration and example for purposes of clarity of understanding, it will be readily apparent to those of ordinary skill in the art in light of the teachings of this invention that certain changes and modifications may be made thereto without departing from the spirit or scope of the appended claims.

    __________________________________________________________________________     SEQUENCE LISTING                                                               (1) GENERAL INFORMATION:                                                       (iii) NUMBER OF SEQUENCES: 2                                                   (2) INFORMATION FOR SEQ ID NO:1:                                               (i) SEQUENCE CHARACTERISTICS:                                                  (A) LENGTH: 1848 base pairs                                                    (B) TYPE: nucleic acid                                                         (C) STRANDEDNESS: single                                                       (D) TOPOLOGY: linear                                                           (ii) MOLECULE TYPE: cDNA                                                       (ix) FEATURE:                                                                  (A) NAME/KEY: CDS                                                              (B) LOCATION: 34..1845                                                         (xi) SEQUENCE DESCRIPTION: SEQ ID NO:1:                                        GGCGCGGCAGGGCCGGGGCAAGCTGGACGCAGCATGATGCGCGCAGTGTGGGAG54                       MetMetArgAlaValTrpGlu                                                          15                                                                             GCGCTGGCGGCGCTGGCGGCGGTGGCGTGCCTGGTGGGCGCGGTGCGC102                            AlaLeuAlaAlaLeuAlaAlaValAlaCysLeuValGlyAlaValArg                               101520                                                                         GGCGGGCCCGGGCTCAGCATGTTCGCGGGCCAGGCGGCGCAGCCCGAT150                            GlyGlyProGlyLeuSerMetPheAlaGlyGlnAlaAlaGlnProAsp                               253035                                                                         CCCTGCTCGGACGAGAACGGCCACCCGCGCCGCTGCATCCCGGACTTT198                            ProCysSerAspGluAsnGlyHisProArgArgCysIleProAspPhe                               40455055                                                                       GTCAATGCGGCCTTCGGCAAGGACGTGCGCGTGTCCAGCACCTGCGGC246                            ValAsnAlaAlaPheGlyLysAspValArgValSerSerThrCysGly                               606570                                                                         CGGCCCCCGGCGCGCTACTGCGTGGTGAGCGAGCGCGGCGAGGAGCGG294                            ArgProProAlaArgTyrCysValValSerGluArgGlyGluGluArg                               758085                                                                         CTGCGCTCGTGCCACCTCTGCAACGCGTCCGACCCCAAGAAGGCGCAC342                            LeuArgSerCysHisLeuCysAsnAlaSerAspProLysLysAlaHis                               9095100                                                                        CCGCCCGCCTTCCTCACCGACCTCAACAACCCGCACAACCTGACGTGC390                            ProProAlaPheLeuThrAspLeuAsnAsnProHisAsnLeuThrCys                               105110115                                                                      TGGCAGTCCGAGAACTACCTGCAGTTCCCGCACAACGTCACGCTCACA438                            TrpGlnSerGluAsnTyrLeuGlnPheProHisAsnValThrLeuThr                               120125130135                                                                   CTGTCCCTCGGCAAGAAGTTCGAAGTGACCTACGTGAGCCTGCAGTTC486                            LeuSerLeuGlyLysLysPheGluValThrTyrValSerLeuGlnPhe                               140145150                                                                      TGCTCGCCGCGGCCCGAGTCCATGGCCATCTACAAGTCCATGGACTAC534                            CysSerProArgProGluSerMetAlaIleTyrLysSerMetAspTyr                               155160165                                                                      GGGCGCACGTGGGTGCCCTTCCAGTTCTACTCCACGCAGTGCCGCAAG582                            GlyArgThrTrpValProPheGlnPheTyrSerThrGlnCysArgLys                               170175180                                                                      ATGTACAACCGGCCGCACCGCGCGCCCATCACCAAGCAGAACGAGCAG630                            MetTyrAsnArgProHisArgAlaProIleThrLysGlnAsnGluGln                               185190195                                                                      GAGGCCGTGTGCACCGACTCGCACACCGACATGCGCCCGCTCTCGGGC678                            GluAlaValCysThrAspSerHisThrAspMetArgProLeuSerGly                               200205210215                                                                   GGCCTCATCGCCTTCAGCACGCTGGACGGGCGGCCCTCGGCGCACGAC726                            GlyLeuIleAlaPheSerThrLeuAspGlyArgProSerAlaHisAsp                               220225230                                                                      TTCGACAACTCGCCCGTGCTGCAGGACTGGGTCACGGCCACAGACATC774                            PheAspAsnSerProValLeuGlnAspTrpValThrAlaThrAspIle                               235240245                                                                      CGCGTGGCCTTCAGCCGCCTGCACACGTTCGGCGACGAGAACGAGGAC822                            ArgValAlaPheSerArgLeuHisThrPheGlyAspGluAsnGluAsp                               250255260                                                                      GACTCGGAGCTGGCGCGCGACTCGTACTTCTACGCGGTGTCCGACCTG870                            AspSerGluLeuAlaArgAspSerTyrPheTyrAlaValSerAspLeu                               265270275                                                                      CAGGTGGGCGGCCGGTGCAAGTGCAACGGCCACGCGGCCCGCTGCGTG918                            GlnValGlyGlyArgCysLysCysAsnGlyHisAlaAlaArgCysVal                               280285290295                                                                   CGCGACCGCGACGACAGCCTGGTGTGCGACTGCAGGCACAACACGGCC966                            ArgAspArgAspAspSerLeuValCysAspCysArgHisAsnThrAla                               300305310                                                                      GGCCCGGAGTGCGACCGCTGCAAGCCCTTCCACTACGACCGGCCCTGG1014                           GlyProGluCysAspArgCysLysProPheHisTyrAspArgProTrp                               315320325                                                                      CAGCGCGCCACAGCCCGCGAAGCCAACGAGTGCGTGGCCTGTAACTGC1062                           GlnArgAlaThrAlaArgGluAlaAsnGluCysValAlaCysAsnCys                               330335340                                                                      AACCTGCATGCCCGGCGCTGCCGCTTCAACATGGAGCTCTACAAGCTT1110                           AsnLeuHisAlaArgArgCysArgPheAsnMetGluLeuTyrLysLeu                               345350355                                                                      TCGGGGCGCAAGAGCGGAGGTGTCTGCCTCAACTGTCGCCACAACACC1158                           SerGlyArgLysSerGlyGlyValCysLeuAsnCysArgHisAsnThr                               360365370375                                                                   GCCGGCCGCCACTGCCATTACTGCAAGGAGGGCTACTACCGCGACATG1206                           AlaGlyArgHisCysHisTyrCysLysGluGlyTyrTyrArgAspMet                               380385390                                                                      GGCAAGCCCATCACCCACCGGAAGGCCTGCAAAGCCTGTGATTGCCAC1254                           GlyLysProIleThrHisArgLysAlaCysLysAlaCysAspCysHis                               395400405                                                                      CCTGTGGGTGCTGCTGGCAAAACCTGCAACCAAACCACCGGCCAGTGT1302                           ProValGlyAlaAlaGlyLysThrCysAsnGlnThrThrGlyGlnCys                               410415420                                                                      CCCTGCAAGGACGGCGTGACGGGTATCACCTGCAACCGCTGCGCCAAA1350                           ProCysLysAspGlyValThrGlyIleThrCysAsnArgCysAlaLys                               425430435                                                                      GGCTACCAGCAGAGCCGCTCTCCCATCGCCCCCTGCATAAAGATCCCT1398                           GlyTyrGlnGlnSerArgSerProIleAlaProCysIleLysIlePro                               440445450455                                                                   GTAGCGCCGCCGACGACTGCAGCCAGCAGCGTGGAGGAGCCTGAAGAC1446                           ValAlaProProThrThrAlaAlaSerSerValGluGluProGluAsp                               460465470                                                                      TGCGATTCCTACTGCAAGGCCTCCAAGGGGAAGCTGAAGATTAACATG1494                           CysAspSerTyrCysLysAlaSerLysGlyLysLeuLysIleAsnMet                               475480485                                                                      AAAAAGTACTGCAAGAAGGACTATGCCGTCCAGATCCACATCCTGAAG1542                           LysLysTyrCysLysLysAspTyrAlaValGlnIleHisIleLeuLys                               490495500                                                                      GCGGACAAGGCGGGGGACTGGTGGAAGTTCACGGTGAACATCATCTCC1590                           AlaAspLysAlaGlyAspTrpTrpLysPheThrValAsnIleIleSer                               505510515                                                                      GTGTATAAGCAGGGCACGAGCCGCATCCGCCGCGGTGACCAGAGCCTG1638                           ValTyrLysGlnGlyThrSerArgIleArgArgGlyAspGlnSerLeu                               520525530535                                                                   TGGATCCGCTCGCGGGACATCGCCTGCAAGTGTCCCAAAATCAAGCCC1686                           TrpIleArgSerArgAspIleAlaCysLysCysProLysIleLysPro                               540545550                                                                      CTCAAGAAGTACCTGCTGCTGGGCAACGCGGAGGACTCTCCGGACCAG1734                           LeuLysLysTyrLeuLeuLeuGlyAsnAlaGluAspSerProAspGln                               555560565                                                                      AGCGGCATCGTGGCCGATAAAAGCAGCCTGGTGATCCAGTGGCGGGAC1782                           SerGlyIleValAlaAspLysSerSerLeuValIleGlnTrpArgAsp                               570575580                                                                      ACGTGGGCGCGGCGGCTGCGCAAGTTCCAGCAGCGTGAGAAGAAGGGC1830                           ThrTrpAlaArgArgLeuArgLysPheGlnGlnArgGluLysLysGly                               585590595                                                                      AAGTGCAAGAAGGCCTAG1848                                                         LysCysLysLysAla                                                                600                                                                            (2) INFORMATION FOR SEQ ID NO:2:                                               (i) SEQUENCE CHARACTERISTICS:                                                  (A) LENGTH: 604 amino acids                                                    (B) TYPE: amino acid                                                           (D) TOPOLOGY: linear                                                           (ii) MOLECULE TYPE: protein                                                    (xi) SEQUENCE DESCRIPTION: SEQ ID NO:2:                                        MetMetArgAlaValTrpGluAlaLeuAlaAlaLeuAlaAlaValAla                               151015                                                                         CysLeuValGlyAlaValArgGlyGlyProGlyLeuSerMetPheAla                               202530                                                                         GlyGlnAlaAlaGlnProAspProCysSerAspGluAsnGlyHisPro                               354045                                                                         ArgArgCysIleProAspPheValAsnAlaAlaPheGlyLysAspVal                               505560                                                                         ArgValSerSerThrCysGlyArgProProAlaArgTyrCysValVal                               65707580                                                                       SerGluArgGlyGluGluArgLeuArgSerCysHisLeuCysAsnAla                               859095                                                                         SerAspProLysLysAlaHisProProAlaPheLeuThrAspLeuAsn                               100105110                                                                      AsnProHisAsnLeuThrCysTrpGlnSerGluAsnTyrLeuGlnPhe                               115120125                                                                      ProHisAsnValThrLeuThrLeuSerLeuGlyLysLysPheGluVal                               130135140                                                                      ThrTyrValSerLeuGlnPheCysSerProArgProGluSerMetAla                               145150155160                                                                   IleTyrLysSerMetAspTyrGlyArgThrTrpValProPheGlnPhe                               165170175                                                                      TyrSerThrGlnCysArgLysMetTyrAsnArgProHisArgAlaPro                               180185190                                                                      IleThrLysGlnAsnGluGlnGluAlaValCysThrAspSerHisThr                               195200205                                                                      AspMetArgProLeuSerGlyGlyLeuIleAlaPheSerThrLeuAsp                               210215220                                                                      GlyArgProSerAlaHisAspPheAspAsnSerProValLeuGlnAsp                               225230235240                                                                   TrpValThrAlaThrAspIleArgValAlaPheSerArgLeuHisThr                               245250255                                                                      PheGlyAspGluAsnGluAspAspSerGluLeuAlaArgAspSerTyr                               260265270                                                                      PheTyrAlaValSerAspLeuGlnValGlyGlyArgCysLysCysAsn                               275280285                                                                      GlyHisAlaAlaArgCysValArgAspArgAspAspSerLeuValCys                               290295300                                                                      AspCysArgHisAsnThrAlaGlyProGluCysAspArgCysLysPro                               305310315320                                                                   PheHisTyrAspArgProTrpGlnArgAlaThrAlaArgGluAlaAsn                               325330335                                                                      GluCysValAlaCysAsnCysAsnLeuHisAlaArgArgCysArgPhe                               340345350                                                                      AsnMetGluLeuTyrLysLeuSerGlyArgLysSerGlyGlyValCys                               355360365                                                                      LeuAsnCysArgHisAsnThrAlaGlyArgHisCysHisTyrCysLys                               370375380                                                                      GluGlyTyrTyrArgAspMetGlyLysProIleThrHisArgLysAla                               385390395400                                                                   CysLysAlaCysAspCysHisProValGlyAlaAlaGlyLysThrCys                               405410415                                                                      AsnGlnThrThrGlyGlnCysProCysLysAspGlyValThrGlyIle                               420425430                                                                      ThrCysAsnArgCysAlaLysGlyTyrGlnGlnSerArgSerProIle                               435440445                                                                      AlaProCysIleLysIleProValAlaProProThrThrAlaAlaSer                               450455460                                                                      SerValGluGluProGluAspCysAspSerTyrCysLysAlaSerLys                               465470475480                                                                   GlyLysLeuLysIleAsnMetLysLysTyrCysLysLysAspTyrAla                               485490495                                                                      ValGlnIleHisIleLeuLysAlaAspLysAlaGlyAspTrpTrpLys                               500505510                                                                      PheThrValAsnIleIleSerValTyrLysGlnGlyThrSerArgIle                               515520525                                                                      ArgArgGlyAspGlnSerLeuTrpIleArgSerArgAspIleAlaCys                               530535540                                                                      LysCysProLysIleLysProLeuLysLysTyrLeuLeuLeuGlyAsn                               545550555560                                                                   AlaGluAspSerProAspGlnSerGlyIleValAlaAspLysSerSer                               565570575                                                                      LeuValIleGlnTrpArgAspThrTrpAlaArgArgLeuArgLysPhe                               580585590                                                                      GlnGlnArgGluLysLysGlyLysCysLysLysAla                                           595600                                                                         __________________________________________________________________________ 

What is claimed is:
 1. An isolated netrin comprising the amino acid sequence of SEQ ID NO:2. 